| Identification | Back Directory | [Name]
CINIDON-ETHYL | [CAS]
142891-20-1 | [Synonyms]
CINIDON-ETHYL
cinidon-ethyl (iso)
Cinidon-ethyl Standard
CIS-ETHYL 2-CHLORO-3-[2-CHLORO-5-(1,3,4,5,6,7-HEXAHYDRO-1,3-DIOXO-2H-ISOINDOL-2-YL)PHENYL]-2-PROPENOATE
2-Propenoic acid, 2-chloro-3-[2-chloro-5-(1,3,4,5,6,7-hexahydro-1,3-dioxo-2H-isoindol-2-yl)phenyl]-, ethyl ester, (2Z)- | [Molecular Formula]
C19H17Cl2NO4 | [MDL Number]
MFCD03095703 | [MOL File]
142891-20-1.mol | [Molecular Weight]
394.25 |
| Chemical Properties | Back Directory | [Boiling point ]
573.7±50.0 °C(Predicted) | [density ]
1.42±0.1 g/cm3(Predicted) | [storage temp. ]
0-6°C | [form ]
neat | [pka]
-2.16±0.20(Predicted) | [BRN ]
8446817 | [Major Application]
agriculture
environmental | [InChI]
1S/C19H17Cl2NO4/c1-2-26-19(25)16(21)10-11-9-12(7-8-15(11)20)22-17(23)13-5-3-4-6-14(13)18(22)24/h7-10H,2-6H2,1H3/b16-10- | [InChIKey]
NNKKTZOEKDFTBU-YBEGLDIGSA-N | [SMILES]
CCOC(=O)\C(Cl)=C\c1cc(ccc1Cl)N2C(=O)C3=C(CCCC3)C2=O |
| Safety Data | Back Directory | [Hazard Codes ]
Xi,N | [Risk Statements ]
43-50/53 | [Safety Statements ]
36/37-60-61 | [RIDADR ]
UN3077 9/PG 3 | [WGK Germany ]
2 | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Aquatic Acute 1
Aquatic Chronic 1
Carc. 2
Skin Sens. 1 |
| Hazard Information | Back Directory | [Description]
Cinidon-ethyl is a post-emergence herbicide. It has a low aqueous solubility, is relatively volatile with a low tendency to leach to groundwater. It is slightly mobile. It is not persistent in soil or water systems. Cinidon-ethyl has a low mammalian toxicity and is not expected to bioaccumulate. It is moderately toxic to earthworms but more toxic to aquatic organisms. It is relatively non- toxic to honeybees. | [Uses]
Herbicide. | [Definition]
ChEBI: Cinidon ethyl is a carboxylic ester and organochlorine compound that is the ethyl ester of cinidon. It has a role as a herbicide. It is a member of isoindoles, a member of monochlorobenzenes and an ethyl ester. | [Production Methods]
Cinidon-ethyl is produced commercially through a multi-step synthesis involving aromatic substitution and esterification reactions. The process begins with the preparation of a substituted phthalimide intermediate, which is then coupled with a chlorinated phenylpropenoic acid derivative. This coupling forms the core structure of cinidon-ethyl. The final step involves esterification with ethanol to enhance solubility and formulation stability. The synthesis is carried out under controlled conditions to ensure high purity and yield. | [Mechanism of action]
Contact action, selective and acts by protox-inhibition | [Pesticide Type]
Herbicide |
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| Company Name: |
Energy Chemical
|
| Telephone: |
021-58432009 400-005-6266 |
| Website: |
http://www.energy-chemical.com |
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